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Health System RADIOLOGY RESEARCH Henry Ford NERS/BIOE 481 Lecture 02 Radiation Physics Michael Flynn, Adjunct Prof Nuclear Engr & Rad. Science [email protected] [email protected]

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Page 1: NERS/BIOE 481 Lecture 02 Radiation Physicsners580/ners-bioe_481/lectures/charts/slides/ners... · NERS/BIOE 481 Lecture 02 Radiation Physics ... • ICRU reports 37 (1984) and 49

Health System

RADIOLOGY RESEARCH

Henry Ford

NERS/BIOE 481

Lecture 02Radiation Physics

Michael Flynn, Adjunct Prof

Nuclear Engr & Rad. Science

[email protected]

[email protected]

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II.A – Properties of Materials (6 charts)

A) Properties of Materials

1) Atoms

2) Condensed media

3) Gases

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II.A.1 – Atoms

• The primary components of thenucleus are paired protons andneutrons.

• Because of the coulomb forcefrom the densely packedprotons, the most stableconfiguration often includesunpaired neutrons

Neutronsneutral charge1.008665 AMU

Protons+ charge1.007276 AMU

Electrons- charge0.0005486 AMU

Positrons+ charge0.0005486 AMU

C136

Carbon 1313 nucleons6 protons7 neutrons

-

+

Terminology

���

A = no. nucleons

Z = no. protons

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II.A.1 – Atoms – the Bohr model

• The Bohr model of the atomexplains most radiation imagingphenomena.

• Electrons are described asbeing in orbiting shells:

• K shell: up to 2 e-, n=1

• L shell: up to 8 e-, n=2

• M shell: up to 18 e-, n=3

• N shell: up to 32 e-, n=4

• The first, or K, shell is the mosttightly bound with the smallestradius. The binding energy(Ionization energy in eV)neglecting screening is ……. )( 22

0 nZII

C136-

--

-

-

-

eV

Niels Bohr (1913). "On the Constitution of Atoms and Molecules, Part I“, Philosophical Magazine 26 (151): 1–24.

Niels Bohr (1913). "On the Constitution of Atoms and Molecules, Part II“, Philosophical Magazine 26 (153): 476-502.

Niels Bohr (1913). "On the Constitution of Atoms and Molecules, Part III“, Philosophical Magazine 26 (155): 857-875.

60.130 I

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II.A.2 – Condensed media

• For condensed material, themolecules per cubic cm can bepredicted from Avogadro’snumber (atoms/cc)

ANN am

• Consider copper with oneatom per molecule,

A = 63.50

r = 8.94 gms/cc

Ncu = 8.47 x 1022 #/cc

• If we assume that the copper atomsare arranged in a regular array, we candetermine the approximate distancebetween copper atoms (cm);

8

31 103.21

Cu

CuN

lcm

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II.A.2 – radius of the atom

•The Angstrom originated as a unit appropriate fordescribing processes associated with atomicdimensions. 1.0 Angstroms is equal to 10-8 cm. Thus theapproximate spacing of Cu atoms is 2.3 Angstroms.

• In relation, the radius of the outer shell electrons(M shell) for copper can be deduced from theunscreened Bohr relationship (Angstroms);

Angstromsr

r

Znr

Cu

Cu

Hm

,16.

29352917. 2

2

Thus for this model of

copper, the atoms constitutea small fraction of the space,

VCu = (4/3)p0.163 = .017 A3

VCu / (2.33) = .001

aH is the ‘Bohr radius’, the radius ofthe ground state electron for Z = 1

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II.A.3 – the ideal gas law

• An ideal gas is defined as one in

which all collisions between atoms

or molecules are perfectly elastic

and in which there are no

intermolecular attractive forces.

One can visualize it as a collection

of perfectly hard spheres which

collide but which otherwise do not

interact with each other.

• An ideal gas can be characterized

by three state variables: absolute

pressure (P), volume (V), and

absolute temperature (T). The

relationship between them may be

deduced from kinetic theory and is

called the “ideal gas law”.

NkTnRTPV P = pressure, pascals(N/m2)

V = volume, m3

n = number of moles

T = temperature, Kelvin

R = universal gas constant

= 8.3145 J/mol.K(N.m/mol.K)

N = number of molecules

k = Boltzmann constant

= 1.38066 x 10-23 J/K

= 8.617385 x 10-5 eV/K

k = R/NA

NA = Avogadro's number

= 6.0221 x 1023 /mol

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II.A.3 – air density

•The density of a gas canbe determined bydividing both sides ofthe gas equation by themass of gas contained inthe volume V.

r = (P/T)/Rg

•The gas constant for aspecific gas, Rg, is theuniversal gas constantdivided by the grams permole, m/n.

Rg = R / (m/n)

• m/n is the atomic weight.

TRP

TRm

n

m

VP

nRTPV

g

Dry Air example

Molar weight of dry air = 28.9645 g/mol

Rair = (8.3145/28.9645) =.287 J/g.K

Pressure = 101325 Pa (1 torr, 760 mmHg)

Temperature = 293.15 K (20 C)

Density = 1204 (g/m3) = .001204 g/cm3

Note: these are standard temperature andpressure, STP, conditions.

gRRm

n

Rg = specific gas constant

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II.B – Properties of Radiation (3 charts)

B) Properties of Radiation

1) EM Radiation

2) Electrons

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II.B.1 – EM radiation

• The electric and magnetic fields are perpendicular to eachother and to the direction of propagation.

• X-ray and gamma rays are both EM waves (photons)

• Xrays – produced by atomic processes

• Gamma rays – produced by nuclear processes

• The energy of an EM radiation wave packet (photon) isrelated to the wavelength;

• E = 12.4/l , for E in keV & l in Angstrom

• E = 1.24/l , for E in keV & l in nm

• E = 1240/l , for E in eV & l in nm

Electromagnetic radiationinvolves electric andmagnetic fields oscillatingwith a characteristicfrequency (cycles/sec)and propagating in spacewith the speed of light.

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II.B.1 – EM radiation

The electromagnetic spectrum covers a wide range of wavelengths

and photon energies. Light used to "see" an object must have a

wavelength about the same size as or smaller than the object.

Lawrence Berkeley Lab: www.lbl.gov/MicroWorlds/ALSTool/EMSpec/EMSpec2.html

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II.B.2 – electron properties

• The electron is one of a class of subatomic particlescalled leptons which are believed to be “elementaryparticles”. The word "particle" is somewhatmisleading however, because quantum mechanicsshows that electrons also behave like a wave.

• The antiparticle of an electron is the positron,which has the same mass but positive rather thannegative charge.

http://en.wikipedia.org/wiki/Electron

•Mass-energy equivalence = 511 keV

•Molar mass = 5.486 x 10-4 g/mol

•Charge = 1.602 x 10-19 coulombs

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II.C – Radiation Interactions (C.1 7 charts)

C) Radiation Interactions

1) Electrons

2) Photons

a. Interaction cross sections

b. Photoelectric interactions

c. Compton scattering (incoherent)

d. Rayleigh scattering (coherent)

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II.C.1 – Electron interactions

Basic interactions of electrons and positrons with matter.

Ee

Elastic Scattering

Ee

Ee

Bremsstrahlung (radiative)

W

E - W

Ee

Inelastic Scattering

Ee - W

W - Ui

Ep

Positron Annihilation

511 keV

511 keV

++-X

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PENELOPE

• Tungsten

• 10mm x 10mm

• 100 keV

For take-offangles of

17.5o-22.5o

0.0006 of theelectronsproduce anemitted x-rayof some energy.

Numerous elasticand inelasticdeflections causethe electron totravel in atortuous path.

II.C.1 – Electron multiple scattering

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II.C.1 – Electron path

• A very large number of interactions with typicallysmall energy transfer cause gradual energy loss asthe electron travels along the path of travel.

1 10 100 10001

10Molybdenum(42)

Tungsten(74)

Me

V/(

g/c

m2)

keV

Electron Stopping Power

http://physics.nist.gov/PhysRefData/Star/Text/ESTAR.html

•The ContinuousSlowing DownApproximation (CSDA)describes the averageloss of energy oversmall path segments.

• ICRU reports 37 (1984)and 49 (1993).

• Berger & Seltzer, NBS82-2550A, 1983.

• Bethe, Ann. Phys., 1930

~E-0.65

MeV/(g/cm2) - For radiation interaction data, units of distance are often scaled usingthe material density, distance * density, to obtain units of g/cm2.

dE/ds

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10 100

1E-3

0.01

0.1

Molybdenum(42)

Tungsten(74)

CSDA Pathlength

path

len

gth

/de

nsit

y(g

m/c

m2)

keV

II.C.1 – Electron pathlength (CSDA)

The total pathlength traveled by the electron along thepath of travel is obtained by integrating the inverse ofthe stopping power, i.e. 1/(dE/ds) ,

gm/cm2

Pathlength is oftennormalized as theproduct of the length incm and the materialdensity in gm/cm3 toobtain gm/cm2.

CSDA –

Continuous SlowingDown Approximation.

dE

dsdE

RT

CSDA 0 1

• 100 keV, Tungsten, 15.4 mm

• 30 keV, Molybdemun, 3.2 mm

~E1.63

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II.C.1 – Electron transport

• A beam of many electrons striking a target willdiffuse into various regions of the material.

50 e

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• Electrons are broadlydistributed in depth, Z,as they slow down dueto extensive scattering.

• Most electrons tend torapidly travel to themean depth and diffusefrom that depth.

Electron Depth Distribution100 keV Tunsten(Penelope MC)

0

0.005

0.01

0.015

0.02

0.025

0.03

0.035

0.04

0.00 1.00 2.00 3.00 4.00 5.00 6.00 7.00

microns

P(z

)dz

50 keV

60 keV

70 keV

80 keV

90 keV

Pz(T,Z) is thedifferential probability(1/cm) of that anelectron within thetarget is at depth Z

II.C.1 – Electron depth distribution vs T

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II.C.1 – Electron extrapolated range

The extrapolated range is commonly measured from electrontransmission data measured with foils of varying thickness. It isdefined as the point where the tangent at the steepest point on thealmost straight descending portion of the penetration curve.

21 /eR gm cm

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II.C.1 – Electron extrapolated range

• The extrapolated range in units of gm/cm2is nearly independent of atomic number.

• The extrapolated range is about 30-40%of the CSDA pathlength.

Tabata, NIM Phys. Res. B, 1996

10 1001E-4

1E-3

0.01

Molybdenum(42)

Tungsten(74)

Extrapolated Range

ran

ge

/den

sit

y(g

m/c

m2 )

keV10 100

0

1

Molybdenum(42)

Tungsten(74)

Extrapolated rangeas a fraction of

CSDA Pathlength

Ra

ng

e/P

ath

len

gth

keV

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II.C – Radiation Interactions (C.2 18 charts)

C) Radiation Interactions

1) Electrons

2) Photons

a. Interaction cross sections

b. Photoelectric interactions

c. Compton scattering (incoherent)

d. Rayleigh scattering (coherent)

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II.C.2.a – Cross sections

• The probability of a specificinteraction per atom is known

as the cross section, s.

• The probability is expressed asan effective area per atom.

• The ‘barn’ is a unit of areaequal to 10-24 cm2 (non SI unit).

• The probability per unit thickness that aninteraction will occur is the product of the crosssection and the number of atoms per unit volume.

μ = s N , (cm2/atom).(atoms/cm3) = cm-1

N = Na (r /A) Na - Avogadro’s # (6.022 x 1023)r - densityA - Atomic Weight

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II.C.2.a – Cross sections for specific materials

• Cross section values aretabulated for theelements and manycommon materials.

• Values range from 101-104 barns (10 to 100keV) depending on Z.

• Cross sections aretypically small relativeto the area of the atom.

Molybdenum

MeV

Barnsatom

http://physics.nist.gov/PhysRefData/Xcom/Text/XCOM.html

Cu, 30 keV

s = 1.15 x 103 b/atom

ACu = 8.04 x 106 b/atom

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II.C.2.a – Linear attenuation coefficients

• The probability per unitthickness that an x-ray willinteract when traveling asmall distance called the‘linear attenuationcoefficient’.

• For a beam of x-rays, therelative change in thenumber of x-rays isproportional to the incidentnumber.

• For a thick object ofdimension x, the solution tothis differential equation isan exponential expressionknown as Beer’s law.

NdX

dN

X

N

DX

N - DNN

xx eNN )0()(

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II.C.2.a – Xray Interaction types

Attenuation is computed from Beer’s law using the linear attenuation

coefficient, m, computed from cross sections and material composition.

Photoelectric effect Coherent scatter

μPE = N1σ 1PE + N2σ 2PE + N3σ 3PE

Where Ni is the number of atoms of type i

and si is the cross section for type i atoms.

xo eNN

In the energy range of interest for diagnostic xray imaging, 10 – 250 keV,there are three interaction processes that contribute to attenuation.

μ = μPE + μINC + μCOH

Incoherent scatter

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II.C.2.b – Photoelectric Absorption

Photoelectric Absorption

• The incident photon transfers all ofit’s energy to an orbital electron anddisappears.

• The photon energy must be greaterthan the binding energy, I, forinteraction with a particular shell.This cause discontinuities inabsorption at the various I values.

• An energetic electron emerges fromthe atom;

Ee = Eg – I• Interaction is most probable for the

most tightly bound electron. A K shellinteraction is 4-5 times more likelythan an L shell interaction.

• Very strong dependance on Z and E.

Photoelectric effect

3

4

E

Z

Akpe

60.13

)(

0

220

I

nZII

eV

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II.C.2.b – Photoelectric Cross Section vs E

Atomic photoelectric cross sections for carbon, ironand uranium as functions of the photon energy E.

from Penelope, NEA 2003 workshop proceedings

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II.C.2.c – Compton Scattering

Compton Scattering

• An incident photon of

energy Eg interactswith an electron with areduction in energy, E’g,and change in direction.(i.e. incoherent scattering)

• The electron recoilsfrom the interaction inan opposite direction

with energy Ee.

Incoherent scatter

-Eg

E’g

Ee

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II.C.2.c – Compton Scattering – energy transfer

The scattered energyas a fraction ofincident energydepends on the angleand scaled energy, a.

Barrett, pg 322

Incident Energy, Eg , MeV

(E’g / Eg)

)(511

cos1111

2

2

keVcm

cm

E

EEE

o

o

cos11

1

E

E

-

q

fEg

E’g

Ee

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Since Z/A is about 0.5 for all but verylow Z elements, the mass attenuation

coeffient, mc/r , is essentially thesame for all materials !

II.C.2.c – Compton Scattering – cross section

• The cross section for compton scattering is expressed as theprobability per electron such that the attenutation coefficientfor removal of photons from the primary beam is;

co

ce

c

A

ZNn

• The Klein-Nishina equation describes thecompton scattering cross section in relationto a classical cross section for photonscattering that is independent of energy(so , Thomson free electron cross section).

)( KNoc f

222

2

21

311

2

1)21ln(

21

12

4

3)(

KNf

Barret, App. C, pg 323

so=(8p /3) re2

re=e2/(moc2)

so= 0.6652 barn

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II.C.2.c – Compton Scattering – cross section vs E

• The free electroncompton scatteringcross section is slowlyvarying with energy forlow photon energies.

• At high energy, a > 1,the cross section is

proportional to 1/E.

Barret, App. C, pg 323

E, MeV

cm2

• The total scattering cross section is made of twocomponent probabilities, sen and ss, describing how muchof the photon energy is absorbed by recoil electrons andhow much by the scattered photon. This difference isimportant in computations of dose and exposure.

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II.C.2.c – Compton Scattering – cross section vs E

• The differential scatteringcross section describes theprobability that the scatteredphoton will be deflected into athe differential solid angle, dW,in the direction (q,f).

• The cross section is forwardpeaked at high energies.

Barret, App. C, pg 326

In the next lecture, we willlearn more about solid angleintegrals. Since the differentialcross for unpolarized photonsdepends only on q, we will find,

dd

d cc sin2

0

d

d c

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II.C.2.c – Compton vs Photoelectric

Photoelectric

Dominant forhigh Z at lowenergy.

Compton

Dominant for lowZ at mediumenergy.

Pair production

Dominant forhigh Z at veryhigh energy.

0.01 0.10 1.00 10.0 100

100

80

60

40

20

0

COMPTON

PHOTO PAIR

Z

MeV

In the field of a nucleus,a photon may annihilatewith the creation of anelectron and a positron.

Eg > 2 x 511 keV

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II.C.2d – Rayleigh Scattering

Rayleigh Scattering

• An incident photon of

energy Eg interactswith atomic electronswith a change indirection but noreduction in energy.(i.e. coherent scattering)

Coherent scatter

Eg

Eg

The Thomson cross section can be understood as a dipole interaction of anelectromagnetic wave with a stationary free electron. The electric field of theincident wave (photon) accelerates the charged particle which emits radiationat the same frequency as the incident wave. Thus the photon is scattered.

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II.C.2d – Rayleigh ScatteringIn the energy range from 20 – 150 keV,coherent scattering contributes 10% - 2% tothe water total attenuation coefficient.

1.00E-04

1.00E-03

1.00E-02

1.00E-01

1.00E+00

1.00E+01

1.00E+02

1.00E+03

1.00E+04

1 10 100 1,000keV

Xray Attenuation Coefficients for Water (cm2/g XCOM)

Rayleigh Scattering (COH)

Compton Scattering (INC)

Photoelectric Absorption

Total (with COH)

20 to 150 keV

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II.C.2d – Rayleigh Scattering

Rayleigh Scattering

• Rayleigh scattering is the coherent interaction of photons with thebound electrons in an atom. The angular dependence is described by

the differential cross section, dsR/dW.

• It is common to consider coherent scattering as a modification, withan atomic form factor, F(c, Z) , of the Thomson cross section,

• For the differential Thomson cross section per electron,

• It depends on the classical electron radius, re2 = 0.079b (slide 30).

• When integrated, the total cross section is the same as so (slide 30).

• The angular distribution is the same as for low energy Compton scattering (slide 32).

• The total cross section is then given by,

Even though there are other components to the totalcoherent scattering, such as nuclear Thomson, Delbruck,and resonant nuclear scattering, Rayleigh scattering isthe only significant coherent event for keV photons.

� � �� Ω

= � � , � �� � � �� Ω

� = sin1

2� ��

� � � �� Ω

=1

2� �� 1 + cos � �

� � = � � �� � � � , � �

� �

1 + cos � � � cos �

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II.C.2d – Rayleigh Scattering

� � = � � �� � � � , � �

� �1 + cos � � � cos �

At low values of c (small angle, low energy)the form factor is equal to the number ofelectrons (i.e 6 for Carbon in this example).

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0.0

0.1

0.1

0.2

0.2

0.3

0.00 10.00 20.00 30.00 40.00 50.00 60.00Theta, degrees

Differential Rayleigh Scattering

dsR/dW= F2(X,Z) dsTh/dWHubbel, J. Phys. Chem. Ref. Data, 1979

6C

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II.C.2d – Rayleigh Scattering

When plotted vs angle, q ,coherent scattering is seento be very forward peaked.

E = 62 keV

l = 0.2 Angstroms

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II.C.2d – Rayleigh Scattering

• Coherent scatteringfrom molecules andcompounds is morecomplex that foratoms.

• King2011 – King BW et. al. ,Phys. Med. Biol, 56, 2011.

• This has beeninvestigated as a wayto obtain materialspecific images.

• Westmore1997 – WestmoreMS et.al., Med.Phys,24,1997

40NERS/BIOE481 - 2018

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II.D – Radiation Interactions (8 charts)

D) X-ray generation

1) Atoms and state transitions

2) Bremmsstralung production

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II.D.1 – Atomic levels

•Each atomic electron occupies a single-particle orbital, withwell defined ionization energy.

•The orbitals with the same principal and total angularmomentum quantum numbers and the same parity make a shell.

C136-

--

-

-

-

Each shellhas a finitenumber ofelectrons,withionizationenergy Ui.

Ka2 , Ka1, Kb2 , Kb1,

from Penelope, NEA 2003 workshop proceedings

a2 a1 b3 b1 b2

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II.D.1 – Atomic relaxation

• Excited ions with a vacancy in aninner shell relax to their groundstate through a sequence ofradiative and non-radiativetransitions.

• In a radiative transition, thevacancy is filled by an electron froman outer shell and an x ray withcharacteristic energy is emitted.

• In a non-radiative transition, thevacancy is filled by an outerelectron and the excess energy isreleased through emission of anelectron from a shell that is fartherout (Auger effect).

• Each non-radiative transitiongenerates an additional vacancy thatin turn, migrates “outwards”.

Radiative

Auger

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II.D.1 – Fluorescent Fraction

Relative probabilities for radiative and Augertransitions that fill a vacancy in the K-shell of atoms.

from Penelope, NEA 2003 workshop proceedings

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II.D.2 – Bremsstralung

• In a bremsstrahlung event, acharged particle with kineticenergy T generates a photonof energy E, with a value inthe interval from 0 to T.

T

Bremsstrahlung (radiative)

E

T- E

• Bremsstrahlung (braking radiation) production results from thestong electrostatic force between the nucleus and the incidentcharged particle.

• The acceleration produced by a nucleus of charge Ze on a

particle of charge ze and mass M is proportional to Zze2/M.Thus the intensity (i.e. the square of the amplitude) will vary as

Z2z2/M2

• For the same energy, protons and alpha particles produce about10-6 as much bremsstrahlung radiation as an electron.

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II.D.2 – Brems. Differential Cross Section (DCS)

• The probability per atom that anelectron traveling with energy T willproduce an x-ray within the energyrange from E to E+dE is known as theradiative differential cross section

(DCS) , dsr/dE.

• Theoretic expressions indicate thatthe bremsstrahlung DCS can beexpressed as;

• Where b is the velocity of theelectron in relation to the speed oflight.

• The slowing varying function,fr(T,E,Z), is often tabulated as thescaled bremsstrahlung DCS.

E

Zf

dE

dZETr

r 12

2,,

e-

EIncidentenergy To

Energy T

Seltzer SM & Berger MJ,

Atomic Data & Nucl. Data Tables,

35, 345-418(1986).

2

22

)1(

11

cmT

e

E

Zf

dE

dZETr

r 12

2

),,(

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II.D.2 – scaled bremsstrahlung DCS

Seltzer and Berger, 1986, from Penelope, NEA 2003 workshop proceedings

Numerical scaled bremsstrahlung energy-loss DCS of Al and Au asa function of x-ray energy relative to electron energy, W/E (E/T).

(mba

rns)

(mba

rns)

Corrected – barns -> mbarns ( i.e. = E/T ) ( i.e. = E/T )

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II.D.2 – angular dependence of DCS

srQ - Barns/nuclei/keV/sr

sr - Barns/nuclei/keV

Q - electron (f,q) – xray (a)

a - xray takeoff angle

(f,q) – electron vector direction

e-E

T =0

To

Q

a

(f,q)

For convenience, the radiative DCS iswritten as,

A doubly differential cross section is usedfor the interaction probability differential inx-ray energy, E, and solid angle, W , in thedirection q ,

The shape function for atomic-fieldbremsstrahlung is defined as the ratio ofthe cross section differential in photonenergy and angle to the cross sectiondifferential only in energy.

And thus,

� � , � , Θ =� � �� �

� � � = � � , � ,Θ � �

� � ≡� � �

� ��

� � � ≡� � � �

� � � Ω�

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II.D.2 – Kissel shape function, S(T,E)

Brems Shape Function100 keV electrons

Molybdenum

0.00

0.05

0.10

0.15

0.20

0.25

0.30

0 20 40 60 80 100 120 140 160 180

Angle (degrees)

S-

(1/s

r)

0

0.1

0.2

0.3

0.4

0.5

0.6

0.7

0.8

0.9

0.95

1

1/4pi

Eg / T

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II.D – Emission of Gamma radiation

In lecture 04 will consider thenuclear processes associated withthe generation of gamma radiation.

a. n/p stability

b. beta emission

c. electron capture

d. positron emission